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EFIPLADIB

Product Name
EFIPLADIB
CAS No.
381683-94-9
Chemical Name
EFIPLADIB
Synonyms
PLA902;PLA 902;PLA-902;EFIPLADIB;Efipladib (PLA 902);4-(3-(1-benzhydryl-5-chloro-2-(2-((3,4-dichlorophenyl)MethylsulfonaMido)ethyl)-1H-indol-3-yl)propyl)benzoic acid;4-(3-(5-chloro-2-(2-(((3,4-dichlorobenzyl)sulfonyl)aMino)ethyl)-1-(diphenylMethyl)-1H-indol-3-yl)propyl)benzoic acid;Benzoic acid, 4-[3-[5-chloro-2-[2-[[[(3,4-dichlorophenyl)methyl]sulfonyl]amino]ethyl]-1-(diphenylmethyl)-1H-indol-3-yl]propyl]-
CBNumber
CB81011218
Molecular Formula
C40H35Cl3N2O4S
Formula Weight
746.14
MOL File
381683-94-9.mol
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EFIPLADIB Property

Boiling point:
891.2±75.0 °C(Predicted)
Density 
1.32±0.1 g/cm3(Predicted)
pka
4.34±0.10(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0019232
Product name
4-(3-(1-BENZHYDRYL-5-CHLORO-2-(2-((3,4-DICHLOROPHENYL)METHYLSULFONAMIDO)ETHYL)-1H-INDOL-3-YL)PROPYL)BENZOIC ACID
Purity
95.00%
Packaging
5MG
Price
$499.62
Updated
2021/12/16
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EFIPLADIB Chemical Properties,Usage,Production

Uses

Treatment of pain and symptomatic management of arthritis.

in vivo

Efipladib (100 mg/kg; p.o.; BID for 31 days) reverses the severity in mouse collagen-induced arthritis (CIA) model[1].
Efipladib (100 mg/kg; p.o.; once) significantly inhibits the nociceptive response 1 h after administration in the rat Complete Freund’s Adjuvant (CFA) nociception model[2].
Efipladib is unable to cross the BBB to gain access to the central compartment[2].
Efipladib (100 nM; IT; 5 μL) reduces PGE2 levels in the cerebrospinal fluid in rats[2].

Animal Model:Mouse collagen-induced arthritis (CIA) model[1]
Dosage:100 mg/kg
Administration:PO, BID for 31 days
Result:Gave a dramatic reduction in the clinical disease severity score relative to the vehicle treated group.
Animal Model:Male Sprague-Dawley rats[2]
Dosage:100 nM in 5 μL of 100% DMSO/rat
Administration:Intrathecal administration
Result:Reduced PGE2 levels in the cerebrospinal fluid (CSF) by 45-60%, yet there was no effect on the nociceptive response.

IC 50

cPLA2α: 0.04 μM (IC50); cPLA2α: 0.067 μM (Ki)

EFIPLADIB Preparation Products And Raw materials

Raw materials

Preparation Products

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EFIPLADIB Suppliers

Tianjin Anhao Biological Technology Co., Ltd.
Tel
Email
sales@ahpharmatech.com
Country
China
ProdList
5734
Advantage
55
Nanjing Shizhou Biology Technology Co.,Ltd
Tel
025-85560043 15850508050
Fax
025-85563444
Email
cindy.huang@synzest.com
Country
China
ProdList
12000
Advantage
58
TargetMol Chemicals Inc.
Tel
15002134094
Email
marketing@targetmol.cn
Country
China
ProdList
29257
Advantage
58

381683-94-9, EFIPLADIBRelated Search:


  • EFIPLADIB
  • 4-(3-(5-chloro-2-(2-(((3,4-dichlorobenzyl)sulfonyl)aMino)ethyl)-1-(diphenylMethyl)-1H-indol-3-yl)propyl)benzoic acid
  • 4-(3-(1-benzhydryl-5-chloro-2-(2-((3,4-dichlorophenyl)MethylsulfonaMido)ethyl)-1H-indol-3-yl)propyl)benzoic acid
  • Efipladib (PLA 902)
  • Benzoic acid, 4-[3-[5-chloro-2-[2-[[[(3,4-dichlorophenyl)methyl]sulfonyl]amino]ethyl]-1-(diphenylmethyl)-1H-indol-3-yl]propyl]-
  • PLA 902
  • PLA902
  • PLA-902
  • 381683-94-9
  • C40H35Cl3N2O4S